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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 9666생성일: 2026년 10월 24일

3-Methylthiophene → Thiophene, 4-methyl-2-[4-(trifluoromethyl)phenyl]-

https://huagongshe.com/ko/reaction/9666

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참여 물질

역할이름HCID투입량
반응물3-MethylthiopheneHCID 12024—
반응물Benzene, 1-bromo-4-(trifluoromethyl)-HCID 67872—
반응물ButyllithiumHCID 178418339—
촉매ZincchlorideHCID 3007855—
촉매Tetrakis(triphenylphosphine)palladiumHCID 11979704—
용매TetrahydrofuranHCID 8028—
생성물Thiophene, 4-methyl-2-[4-(trifluoromethyl)phenyl]-HCID 21986373—

반응 조건

온도0 °C

반응 단계

To a solution of 3-methylthiophene (2.31 ml) in anhydrous THF (75 ml) at −78° C. under N2 was added dropwise n-BuLi (1.6 M in hexanes, 15 ml). Thirty minutes after the addition was complete, the reaction mixture was allowed to warm to 0° C. and stirred for a further 30 minutes. Zinc chloride (0.5 M in THF, 48 ml) was added drop-wise, after a further 15 minutes palladium (0) tetrakis(triphenylphosphine) (100 mg) and 4-bromobenzotrifluoride (3.36 ml) were added and the reaction allowed to attain room temperature. The reaction mixture was warmed to 40° C. and stirred at this temperature for 3 hours. The reaction mixture was then cooled to room temperature and the solvents removed in vacuo. The residue was partitioned between and ether and the aqueous extract further washed with ether. The combined organic extracts were dried (MgSO4), filtered and evaporated to yield a brown oil. Purification by Biotage® chromatography eluting with cyclohexane yielded the title compound as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07091237B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-15ae2bc802194632a49a178c7691a128
출처 메모uspto-grants-2006_08